Giving Tuesday is December 3

Make a generous gift in support of the alopecia areata movement today and it will be matched up to $25,000!

GIVE NOW

Our Thanks to You!

You can still help by making a contribution to the Walk For Alopecia today in support of research and services!

LEARN MORE

New Wig Reimbursement Resource

Tips and tools to help you advocate for insurance coverage, including filing claims and appealing denials.

LEARN MORE

Help for Today, Hope for Tomorrow

Help the alopecia areata community now and for years to come. We are excited to announce our partnership with FreeWill, a complimentary online tool designed to help with your estate planning. You can help support alopecia research, support, and awareness by directing a gift to NAAF through your will or estate plan..

LEARN MORE

Find a Youth Mentor

NAAF’s Youth Mentor Program connects children living with alopecia areata to dedicated young adult mentors to formulate lasting bonds while providing support and guidance on dealing with the day-to-day challenges stemming from alopecia areata.

LEARN MORE

New Wig Resource

Buy 1/Give 1 opportunity thanks to C&S Fashions

LEARN MORE
Two images of one alopecia areata type

What is Alopecia Areata?

Alopecia areata is a common autoimmune disease, causing sudden hair loss on the scalp, face, and sometimes other areas of the body. There are different levels of alopecia areata severity. The three main types of alopecia areata are patchy, alopecia totalis (total hair loss on the scalp), and alopecia universalis (total hair loss on the body).

Learn the facts.

Latest News

#News

LEQSELVI™ Commercial Launch Indefinitely Delayed Due to Patent Ruling

This past July, the U.S. Food and Drug Administration (FDA) approved LEQSELVI™ (deuruxolitinib) for alopecia areata, making it the third…

Learn More
#Advocacy

2nd Annual Walk For Alopecia Exceeds $900,000 Goal

The National Alopecia Areata Foundation (NAAF) is proud to announce its 2nd Annual Walk For Alopecia™ has exceeded its $900,000…

Learn More
#News

Challenges in Alopecia Areata and Opportunity to Drive Change

Last year, Nicole Friedland, NAAF President and CEO, participated in an expert steering committee, the Alopecia Areata Consensus Task Force,…

Learn More
#News

FDA Approves LEQSELVI™ for Adults with Severe Alopecia Areata

Today, the U.S. Food and Drug Administration (FDA) approved LEQSELVI™ (deuruxolitinib) for alopecia areata, marking the third FDA-approved treatment for…

Learn More
#News

NAAF Awards New Research Grants

NAAF awards research grants to researchers with promising proposals to learn more about alopecia areata – what is happening in…

Learn More
#Enews

Exciting New Wig Resource for the Alopecia Areata Community

NAAF is thrilled to announce a new collaboration with C&S Fashions Inc., a company that has been at the forefront…

Learn More
#News

Wig Bills Make Progress in California and New York

This past February, California Assembly Member Marc Berman (D-Menlo Park) introduced AB 2668 – Health Insurance Coverage for Wigs. This…

Learn More
Emma Guttman #News

NAAF Applauds NIH Award to Mount Sinai for Alopecia Areata Research

The National Alopecia Areata Foundation applauds the announcement that the National Institutes of Health (NIH) has awarded a $6.6 million…

Learn More
#News

NAAF Team Attends American Academy of Dermatology Meeting in San Diego

Members of the NAAF team represented the organization and the alopecia areata patient community at the 2024 Annual Meeting of…

Learn More
#News

Dr. Brett King to Speak at NAAF Conference

It was June 2014 when the electrifying news came out of Yale University that a dermatologist named Brett King saw…

Learn More
#Webinars

Upcoming Webinar

Empowered Choices: Navigating Your Alopecia Areata Journey TUESDAY, DECEMBER 17, 2024 4PM…

Register Now!

Get Involved

volunteers at NAAF alopecia areata conference

Be a NAAF Conference Volunteer

Become a NAAF Conference Volunteer NAAF is always looking for enthusiastic volunteers for our annual alopecia areata patient conference. We…

Learn More

Support Groups

Join A Support Group After an alopecia areata diagnosis, it is important to realize that you are not alone. NAAF…

Learn More

One-on-One Phone Support

Would you like some one-on-one phone support? NAAF can help you with that. There are several things you can do…

Learn More

NAAF Youth Mentor Program

Have you heard of the NAAF Youth Mentor Program? Do you have a child or teen with alopecia areata between…

Learn More

Impact

7M

Americans affected by alopecia areata

Research

Largest non-profit funder of alopecia areata research in the world

40+

Years as the VOICE of the alopecia areata community

Welcome to the NAAF Website